A Heart to Remember: Vea's Story - Nemours Blog

COMMUNITY CONNECTION

A Heart to Remember: Vea’s Story

1 min read
Guest Contributor

For the Tsoflias family, the past year has been a roller coaster of emotion, disbelief, heartbreak and ultimately, hope.

It all began when a routine 20-week ultrasound revealed an abnormality. Brittany, an expectant first-time mom, was referred to Nemours Children’s fetal cardiologist, Shubhika Srivastava for a fetal echo and soon learned that her baby had a very rare congenital heart defect called Ebstein’s Anomaly.  The defect is linked to an abnormality in the tricuspid valve, causing it to leak and if left unchecked, would result in heart failure. To correct the defect, surgery would be required. 

Knowing that her baby would need highly specialized heart care immediately after birth, Brittany delivered Vea through the Advanced Delivery Program at Nemours Children’s Hospital, Delaware. “What an amazing experience. I felt special, says Brittany, because everyone went above and beyond for me.”

Recognized as a surgical expert in this type of complex heart defect, Dr. Christian Pizarro, successfully repaired Vea’s heart when she was just 11 months old.

Now, one year after surgery, Vea is thriving and mobile–-crawling like crazy and stealing hearts with her wide-eyed, glance.  It’s possible, Vea may need another surgery at some point and if she does, “we would put our trust in Dr. Pizarro all over again.”

Guest Contributor
Topics: Community Connection
Guest Contributor

Like and follow Nemours on Facebook, Instagram, Twitter, and LinkedIn.

Related Articles

UNCATEGORIZED

A Heart to Remember: Brayden’s Heart Transplant Story

When Brayden was born, he was premature and was having a hard time gaining weight. His family took him to weekly weight checks with little to no change taking place. After a change of pediatricians, they were told he had a heart murmur. Brayden and his family were referred to Nemours Children’s Hospital, Delaware for further evaluation with the cardiac team. Brayden was diagnosed with dilated cardiomyopathy, requiring the initiation of medication to observe his response. With additional testing, the diagnosis of Barth Syndrome was confirmed. Barth Syndrome is a rare condition that causes an enlarged and weakened heart, weakness in muscles, frequent infections, and more. Due to his inability to gain weight, a G-tube, otherwise known as a  Mickey button, was placed to provide extra calories and nutrition to Brayden which overnight feeds. Brayden received yearly cardiac catheterizations to monitor the function of his heart. In December 2014, when […]

FEATURED POST

World Heart Day- Greyson’s Story

Caring for critically ill infants with congenital heart defects using an app Greyson was born at 39 weeks on August 3, 2020, and just 24 hours later arrived home to meet his two, very excited older siblings.  A week later, Greyson wouldn’t eat. His parents, sensing something was wrong, brought him to Nemours Children’s Hospital, Delaware where he was admitted to the intensive care unit and put on oxygen.  At first, doctors thought it was a viral infection, but an echo of Greyson’s heart revealed that he was in heart failure.  The diagnosis was hypoplastic left heart syndrome (HLHS), a severe congenital heart defect, requiring a series of three highly complex surgeries to correct it.  With Greyson just 10 days old, Dr. Christian Pizarro performed the first surgery. All went well.  Greyson spent the next 7 weeks recovering in the hospital and as discharge planning began, acute care pediatric cardiologist, Dr. Erica Del Grippo cautioned his parents that the […]

Patient surrounded by her care team

SERVICES & SPECIALTIES

The Beat Goes On: Grace, a Heart Patient, Shares Her Story

Back in February of 2016, I started experiencing horrible palpitations, and decided one day to go get it to check out. I was immediately diagnosed with (WPW) -Wolff-Parkinson-White syndrome. After my first heart ablation, everything went smoothly. I was back to doing all the sports I loved like track and cheer! I was living life to the fullest. However, a couple of months later, I started to have the same palpitations, along with being super tired and getting dizzy. The doctor I originally went to had moved away, so my mom who is a nurse, did her research, and we decided to switch over to Nemours Children’s Health.  Seeing a cardiologist there, I had my second heart ablation in December 2016. I was 14 years old and have had two heart ablations! The surgery was quick, and I was told that everything looked good, they said. I recovered perfectly and […]